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Alexander disease type II
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Acute myeloid leukemia with CEBPA somatic mutations
1 associated gene
No signs/symptoms info
Alexander disease type II
Acute myeloid leukemia with CEBPA somatic mutations

GFAP
(UniProt - OMIM)
 CEBPA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
GFAP
(0.63)
CEBPA


Citations in the biomedical literature:


Alexander disease type II
GFAP
Acute myeloid leukemia with CEBPA somatic mutations
CEBPA



Alexander disease type II
Acute myeloid leukemia with CEBPA somatic mutations

Synonym(s):
- AxD type II
Synonym(s):
- AML with CEBPA somatic mutations
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: adult
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.